Canonical Allele Identifier: CA132154914
Gene: STK10 HGNC NCBI

Linked Data

dbSNP Id: rs974559281
gnomAD v2: 5-171559444-T-G
gnomAD v3: 5-172132440-T-G
gnomAD v4: 5-172132440-T-G
MyVariant Identifiers: chr5:g.171559444T>G (hg19) chr5:g.172132440T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.172132440T>G , CM000667.2:g.172132440T>G GRCh38
NC_000005.9:g.171559444T>G , CM000667.1:g.171559444T>G GRCh37
NC_000005.8:g.171492049T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000176763.10:c.322-5019A>C MANE Select ENSP00000176763.5:n.322-5019A>C
ENST00000176763.9:c.322-5019A>C ENSP00000176763.5:n.322-5019A>C
ENST00000519710.1:n.103-5019A>C
NM_005990.3:c.322-5019A>C NP_005981.3:n.322-5019A>C
XM_011534641.1:c.322-5019A>C XP_011532943.1:n.322-5019A>C
XM_011534643.1:c.322-5019A>C XP_011532945.1:n.322-5019A>C
XM_011534644.1:c.322-5019A>C XP_011532946.1:n.322-5019A>C
XM_017009788.1:c.-3-5019A>C XP_016865277.1:n.-3-5019A>C
NM_005990.4:c.322-5019A>C MANE Select NP_005981.3:n.322-5019A>C
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